HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Methoxystyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Product | 4-Methoxystyrene | HCID 12507 | — |
Reaction Steps
p-Methoxystyrene was polymerized in the same manner as in Example 10, and 25 ml (0.26 mole/1) of p-tert-butoxystyrene was thereafter added to the reaction mixture and further polymerized therewith at an elevated temperature of 25° C. Subsequently, methanol (330 mmoles/1) containing a small amount of ammonia water was added to the reaction system to terminate the polymerization and obtain a mixture containing a polymer. The mixture was washed first with a hydrochloric acid aqueous solution (8 vol. %) and then with water, followed by evaporation for the removal of the solvent, etc. to collect the polymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102966 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-2c3e7a102e2a464c96695f2ed1365b95 |
| Source note | uspto-grants-1992_04 |